WO2003002645A1

WO2003002645A1 - Adhesion promoter for plastisols

Info

Publication number: WO2003002645A1
Application number: PCT/EP2002/006686
Authority: WO
Inventors: Günter Butschbacher
Original assignee: Henkel Teroson Gmbh
Priority date: 2001-06-27
Filing date: 2002-06-18
Publication date: 2003-01-09
Also published as: US7163976B2; US20040167253A1; EP1406960A1; DE10130888A1

Abstract

The invention relates to plastisols that have good adhesive properties with a large number of substrates used in the automotive industry. The inventive plastisols are obtained by adding pulverulent monosaccharides, disaccharides or oligosaccharides to plastisols on the basis of pulverulent organic polymers and plasticizers. The inventive plastisols are characterized by a good adhesive behavior and excellent aging stability and can be used in the automotive industry both in the body construction as well as in the enameling line and in the trim shop as adhesive, sealing or coating agents.

Description

"Adhesion promoter for plastisols"

The invention relates to plastisol compositions based on powdery organic polymers and plasticizers and adhesion-promoting additives.

Plastisols are generally understood to mean dispersions of organic plastics in plasticizers which gel when heated to a higher temperature and harden when cooled. The plastisols commonly used in practice today mostly contain fine powder homo- or copolymers of vinyl chloride which are dispersed in a liquid plasticizer and form a paste. Such polyvinyl chloride plastisols (PVC plastisols) are used for a wide variety of purposes. They are used, among other things, as sealing compounds, e.g. for seam seals in metal containers or as flanged seam adhesives in the metal industry, as corrosion protection coatings for metals (e.g. as underbody protection for motor vehicles), for impregnating and coating substrates made of textile materials (e.g. as carpet backing), as cable insulation, etc. ). Plastisols based on finely powdered methacrylate copolymers (PMMA) or styrene copolymers have also become known. Such plastisols, in particular those based on PVC or PMMA, are also used extensively in body-in-white construction in the automotive industry. For relining stiffening structures such as bonnets, trunk lids, doors, roof structures, as well as for flanged seam bonding and for sealing seams from other joining processes. Advantageous when using plastisols for these purposes are their favorable flow behavior, especially at room temperature. In order to ensure the laundry resistance in the various cleaning, phosphating and immersion priming stages in the manufacture of the automobile bodies, these plastisol compositions are often gelled in a pre-gelling process to such an extent that their viscosity is high enough to ensure this laundry resistance and an initial strength of the components , Depending on the application, additional additives are added to the plastisols. Such additives are, for example, rheology aids, stabilizers, adhesion promoters, fillers, pigments, blowing agents, reactive (crosslinkable) additives and water-absorbing substances. Adhesion promoters are added to the plastisols in order to ensure long-term adhesion of the plastisols to steel, aluminum or galvanized and / or electrocoated or otherwise pretreated metal sheets. For example, basic compounds such as polyaminoamides (PAA) are used as adhesion promoters for PVC plastisols. For polymethacrylate plastisols, basic vinylimidazoles are usually used as adhesion promoters, which are copolymerized as comonomers. If appropriate, polyaminoamides are added to these PMMA plastisols as an additional adhesion promoter component. Other additives for plastisols are also known.

GB-A-1193896 describes a PVC plastisol which contains an epoxy resin and dicyandiamide and α-benzyldimethyldiamine as adhesion-promoting substances. DE-A-2642514 proposes adding Schiff bases and / or enamines based on polyaminoamides and epoxy resins to the PVC pastisols in order to improve their adhesion to metallic substrates. The use of polyaminoamides and their derivatives and reaction products as adhesion promoters for plastisols, in particular PVC - plastisols is also the subject of a large number of patent applications, examples of which are DE-A-2906134, DE-A-3111815, DE-A-3201265, EP-A - 171850 or EP-A-263053.

Furthermore, the use of blocked diisocyanate polymers either alone or in combination with amine derivatives or polyaminoamide derivatives is proposed as adhesion-promoting substances for plastisols. Examples include EP-A-214495 or US-A-5130402.

US-A-5039768 proposes the use of organosilanes, acrylate monomers, and unsaturated carboxylic acid monomers and epoxy resins with hardeners as adhesion-promoting additives for PVC plastisols. The EP A-343101 proposes the addition of anhydride compounds and epoxy resins to PVC plastisols in order to improve the adhesion. Similarly, EP-A-533026 proposes copolymers of methyl methacrylate with comonomers containing carboxyl or anhydride groups as adhesion promoters for acrylate plastisols, which may optionally contain polyaminoamide additives. EP-A-209653 proposes reaction products of epoxy resins and low molecular weight aliphatic polyamines, in particular ethylenediamine, as adhesion-promoting additives to plastisols, in particular to plastisols based on methyl methacrylate copolymers.

Despite a large number of proposed solutions for achieving good adhesion of plastisol compositions on a wide variety of substrates, in particular metallic substrates, it is desirable to achieve permanent and aging-resistant adhesion of plastisols as cost-effectively as possible, which can be used reliably as a crimp seam adhesive, relining adhesive, seam sealant, as spot welding paste or can also be used as a coating compound, possibly with acoustic properties. The products used in this way should meet high requirements for corrosion protection. The invention is therefore based on the object of providing inexpensive, readily available adhesion-promoting additives for plastisols which meet today's requirements for corrosion protection in automobile construction.

The solution to the problem according to the invention can be gathered from the patent claims; it essentially consists in providing plastisol compositions based on powdered organic polymers and plasticizers which contain powdered monosaccharides, disaccharides or oligosaccharides.

Polyvinyl chloride (PVC), vinyl chloride copolymers with vinyl acetate, styrene and / or alkyl (meth) acrylates, copolymers of styrene with (meth) acrylic acid, (meth) acrylamide and / or alkyl (meth) acrylates or else copolymers can preferably be used as powdered organic polymers of methyl or ethyl methacrylate with C _{3 to} C ₈ alkyl (meth) acrylates or Alkyl (meth) acrylate homopolymers or mixtures of the aforementioned polymers can be used.

As monosaccharides, disaccharides or oligosaccharides, glucose, galactose, mannose, fructose, arabinose, xylose, ribose, 2-deoxy-ribose, cellobiose, maltose (malt sugar), lactose (milk sugar), sucrose (cane sugar) - the latter is particularly good Availability and its low price particularly preferred, Gentiobiose, Melibiose, Trehalose, Turanose, Gentianose, Kestose, Maltotriose, Melecitose, Raffinose, Stachyose, Lychnose, Secalose, or mixtures thereof are used.

The mono-, di- or oligosaccharides are preferably used as finely divided powders, the average particle size should be between 1 and 100 μm, preferably it should be between 1 and 20 μm. It may be expedient to grind the commercially available powdered saccharides more finely, for this purpose, in particular, they can be pasted with the plasticizer to be used in the plastisol, this paste then being rubbed off with conventional colloid mills or on a roller, so that the desired average particle size of the saccharide is achieved becomes.

All conventional plasticizers are generally suitable as plasticizers (see, for example, Paul E. Bruins, Plasticizer Technology [Reinhold Publ. Corp., New York], Vol. 1, pp. 228-232). C ₄ to C ₁₆ alkyl phthalates such as dibutyl phthalate, dioctyl phthalate, diheptyl phthalate, benzyl butyl phthalate, dibenzyl phthalate, diisononyl phthalate (DINP), diisodecyl phthalate (DIDP) and diundecyl phthalate (DIUP) are preferred. However, the known plasticizers from the group of organic phosphates, adipates and sebacates or also benzyl benzoate and other benzoate plasticizers, alkyl sulfonic acid esters of phenol or cresol, dibenzyl toluene or diphenyl ether are also suitable. The selection criteria for the preferred plasticizers depend on the one hand on the polymer composition and on the other hand on viscosity, Gelling conditions of the plastisol and the desired acoustic properties of a plastisol-coated composite.

The plastisols according to the invention can contain further reactive additives, for example di- or polyisocyanates, these preferably being blocked or microencapsulated, and also di- or polyamines or polyaminoamides based on polyamines and dimerized or polymerized fatty acids and / or hydroxy-functional compounds, such as eg Polyester polyols or polyether polyols. Further examples of reactive additives are combinations of di- or polyepoxy compounds in combination with di- or polyamines or polyaminoamides. It is also possible to add monomeric mono-, di- and / or trimethacrylates or -acrylates or polyester resins, which may contain olefinically unsaturated double bonds, in combination with peroxides, although the use of (meth) acrylate monomers is not one of the preferred embodiments of the invention

Plastisol compositions belong to the fact that the addition of the monomeric (meth) acrylates in combination with peroxides often leads to storage stability problems. In addition, the low-temperature flexibility of such compositions is often unsatisfactory because of the high degree of crosslinking. Furthermore, carboxylic acid derivatives, in particular dicarboxylic acids, di- or tricarboxylic acid anhydrides, can be added to the plastisols according to the invention as reactive additives. Concrete examples are adipic acid, pimelic acid anhydride, suberic acid, azelaic acid, sebacic acid, undecanedioic acid, dodecanedioic acid, phthalic acid, maleic anhydride, succinic anhydride, 1, 2,3-Propantricarbonsäure-, phthalic anhydride, anhydrides of the isomeric Benzoltribarbonsäuren, pyromellitic anhydride, methyl-hexahydrophthalic anhydride, and similar common carboxylic acids or their anhydrides. Β-dicarbonyl compounds such as, for example, acetylacetone, acetoacetic ester, dialkyl malonates, benzoyl acetate or corresponding metal chelates such as, for example, zinc acetylacetonate can also be added. The reactive additives are usually used in amounts between 0.01 and 4% by weight, preferably between 0.1 and 20% by weight, based on the entire plastisol formulation.

In addition, the plastisols according to the invention can optionally contain further auxiliaries and additives, as are customary in plastisol technology. These include e.g. Color pigments, anti-aging agents, rheology aids and blowing agents for the production of foamed plastisols. These common additives include, for example, epoxy plasticizers, preferably epoxidized natural oils such as epoxidized soybean oil, epoxidized linseed oil or epoxidized tall oils. As is known, these epoxy plasticizers are used in small quantities, in particular in PVC plastisols, as heat stabilizers. The plastisols can also contain the usual anti-aging agents and stabilizers, rheology aids such as e.g. contain fumed silicas, bentones, castor oil derivatives.

All fillers which are common and known per se in plastisol technology can be used as fillers. Examples of suitable fillers are limestone powder, natural, ground chalk (calcium carbonate or calcium magnesium carbonate), precipitated chalk, heavy spar, talc, mica, clays, pigments such as e.g. Titanium dioxide, carbon black, iron oxides.

Because of the positive properties and the low price, the powdery saccharides can be used in very high proportions in the plastisols according to the invention and thus replace some of the fillers. Therefore, the saccharides can make up up to 50% by weight of the total formulation. Many formulations contain between 3 and 10 or 20% by weight saccharide. Furthermore, so-called “light fillers” of organic or inorganic composition can also be used, these include, for example, hollow glass spheres, fly ash (“fillite”) and organic hollow microspheres based on epoxy resins or phenolic resins. Furthermore, conductivity-imparting pigments such as special carbon blacks, graphite or antimony-doped silicates can be added. This is particularly necessary if the plastisols are applied to the shell and then electrophoretically deposited lacquer layers are to be applied to these plastisol layers.

For the production of specifically light plastisols, so-called hollow microspheres or blowing agents in expanded and unexpanded form can also be added if the plastisols are to be foamed during the gelling process. Suitable blowing agents are all blowing agents known per se, preferably organic blowing agents from the class of azo compounds, N-nitroso compounds, sulfonyl hydrazides or

Sulfonyl. Examples from the class of azo compounds are azobis-isobutyronitrile and in particular azodicarbonamide, from the class of nitroso compounds the di-nitrosopentamethylenetetramine should be mentioned, from the class of sulfohydrazides 4,4'-oxybis (benzenesulfonic acid hydrazide) and from the class of Semicarbazide called the p-toluenesulfonylsemicarbazid.

Another possibility of foaming up the plastisols according to the invention is to add so-called microspheres to the plastisols. Such hollow microspheres can either be added directly to the plastisol in the pre-expanded form as hollow microspheres or, in a particularly preferred manner, the "hollow microspheres" are added to the plastisol as finely divided powder in the unfoamed form. These unfoamed "hollow micro spheres" only expand when the plastisol is gelled and thus result in a very uniform and fine-pored foaming. The hollow microspheres contain a liquid blowing agent based on aliphatic hydrocarbons or fluorocarbons as the core and a shell made of a copolymer of acrylonitrile with vinylidene chloride and / or methyl methacrylate and / or methacrylonitrile. When using such microspheres, the expansion of the microspheres and thus the foaming takes place only during the gelling process of the plastisol. The use of such microspheres is described for example in EP-A-559254. Such "hollow microspheres" are commercially available, for example, under the trade name "Expancel" from Nobel Industries or as "Dualite" from Pierce & Stevens. According to the invention, it is also possible to further improve properties of the plastic gel, in particular the abrasion resistance, by adding to the plastisol a compound which reacts at the gelation temperature with the carboxyl groups of the optionally present copolymers with crosslinking in an amount of up to 40% by weight , Long-chain epoxy compounds, epoxidized polybutadienes or also epoxidized natural oils such as epoxidized soybean oil or solid, powdered epoxy derivatives are particularly suitable for a reaction with the carboxyl groups present. Liquid hydroxy-functional polybutadienes or mercaptan-terminated liquid polymers can also be used instead of or in combination with polypropylene glycols. The formation of ester bonds between these compounds and the carboxyl groups of the copolymer generally takes place when the plastisol is heated to the setting temperature. If necessary, however, suitable catalysts can be added in an amount of about 0.01 to 2.0% by weight, for example imidazole or substituted imidazoles such as N-alkylimidazoles, for example N-methylimidazole, tertiary amines, tetramethylene diamine or urea derivatives, if appropriate precipitated on inert fillers. Alkylbenzenesulfonic acids and titanates are also suitable as catalysts for the ester formation with glycols.

Furthermore, amino and / or amido-functional compounds and / or blocked polyurethanes can be added individually or in combination to the plastisols according to the invention, as are known from the PVC plastisol technology as adhesion promoters, they bring about a considerable improvement in the abrasion resistance. Examples of such compounds are the well known polyaminoamides based on dimerized fatty acids and low molecular weight di or polyamines, e.g. are known under the trade names Versamid 115, 125 or 140 and / or amino-functional condensation products from epoxides based on the bisglycidyl ether of bisphenol A with diamines or polyamines such as e.g. Ethylenediamine, propylenediamine, etc.

Another way to improve the mechanical properties of the plastic gels is that in the plasticizer in polyurethane Form of isocyanate prepolymers and low molecular weight aliphatic or cycloaliphatic diamines dissolves. The isocyanate prepolymers preferably contain blocked isocyanate groups, for example isocyanate groups blocked by caprolactam, or they are in the form of solid, microencapsulated or surface-deactivated isocyanate compounds as a dispersion in the liquid phase. These isocyanate derivatives can be present in an amount of up to 30% by weight of the total formulation, the (cyclo) aliphatic diamines can be up to 5% by weight in the case of low molecular weight amines up to a molecular weight of about 500 and up to 30% by weight in the case of higher molecular weight diamines. make up the overall wording. When heated to the setting temperature, polyurethane formation occurs, whereby the plastisol polymer may form an IPN structure (Interpenetrating Polymer Network).

If another crosslinking comonomer has been polymerized into the copolymer, the plastisols according to the invention can contain further reactive additives to improve the mechanical properties. These depend on the crosslinking comonomer used. In the case of hydroxy-functional comonomers, di- or polyisocyanates can be added, the latter preferably being blocked or microencapsulated; in the case of epoxy-functional comonomers, di- or polyamines or polyaminoamides are preferably added; in the case of (blocked) isocyanate-functional comonomers, amino- and / or hydroxy-functional additives can be used. If appropriate, these crosslinking reactions can be accelerated by catalysts known per se.

The plastisol compositions contain:

a) 5 to 60% by weight of at least one powdered polymer, b) 5 to 65% by weight of plasticizer, c) 0 to 40% by weight of fillers, d) 1 to 30% by weight of at least one mono-, di- or oligosaccharide e) 2 to 40% by weight of reactive additives, selected from the group of optionally blocked or microencapsulated di- or polyisocyanates; amino- and / or hydroxy-functional additives, especially di- or polyamines or polyaminoamides, imidazole derivatives, epoxy resins, condensation products from epoxy resins and polyaminoamides and / or di- or polyamines, dicarboxylic acids, di- or tricarboxylic acid anhydrides, acetylacetonates, peroxides or mixtures of the aforementioned reactive additives f) If necessary, further auxiliaries and additives, the sum of the individual components being 100% by weight.

The use of saccharides as an adhesion-promoting additive has the following advantages over the known prior art: improved resistance to aging, especially after

Salt spray test according to DIN 50021, the VDA test (VDA 621-415), the

Splash water test or combinations of these tests, reduced tendency to bubble after moisture absorption,

Use of renewable raw materials, low material costs free of toxic heavy metals, therefore toxicologically harmless and environmentally friendly.

In the case of methacrylate plastisols in particular, the addition of graphite can be dispensed with, if desired, and nonetheless aging-resistant formulations are achieved, which has previously only been possible with the addition of graphite.

The plastisol compositions according to the invention have good adhesion properties on a wide variety of substrates such as steel, electrolytically galvanized steel, hot-dip galvanized steel or organically coated steel ("Granocoat" or "Bonazink"). According to the current state of the art, aging-resistant adhesion and good corrosion protection were only possible by adding - often containing heavy metals - corrosion protection pigments and / or corrosion inhibitors. The plastisols according to the invention are suitable as adhesives, in particular as so-called structural adhesives, but also for underbody protection, for seam sealing, for relining engine hoods, trunk lids, doors or, if pre-gelling is used, also as a roof bow. Furthermore, the plastisols according to the invention are suitable for seam sealing, as a flanged seam adhesive, for flared seam sealing or as a spot welding paste. Because of the good adhesive properties on a large number of substrates, the plastisols according to the invention can therefore be used both in body-in-white, as well as in the lacquer area or in the trim area in the manufacture of automobiles. Underbody application on raw sheet metal is also possible.

The following examples are intended to explain the invention in more detail; they are only exemplary in nature and do not cover the entire breadth of the plastisols according to the invention. From the above However, the person skilled in the art can easily derive information from the entire range of applications.

Examples

Example 1: (comparison)

Flare seam adhesive and flare seam sealing based on a PVC plastisol: In the following case, a basic approach according to the state of the art used corrosion protection pigment or powdered sugar according to the invention:

Example 2: (according to the invention)

Example 3: (According to the invention) commercially available underbody protection to which 10% cane sugar was added.

Example 4: (Comparison) standard underbody protection.

Example 5

Underbody protection based on PMMA

Example 6:

Underbody protection based on PMMA without dextrose

Compared to comparative example 1, example 2 according to the invention shows good results in all layer thicknesses of the coating after short-term gelation at high temperatures, followed by moisture storage. In no case blistering is observed in the coating, whereas blistering is frequently observed with the adhesive according to the prior art. In addition, the strontium-containing corrosion protection pigment can be dispensed with in the example according to the invention.

Example 3 according to the invention shows an underbody protection which contains sucrose in large amounts, partly as a filler, so that the proportion of specifically heavy calcium carbonate could be drastically reduced. This enables a specifically light underbody protection which is absolutely equal in its adhesion behavior to a specifically heavier commercially available underbody protection with a high proportion of calcium carbonate (example 4).

In the same way, the underbody protection according to the invention based on PMMA of Example 5 results in a specifically particularly light underbody protection, since it was also possible to dispense with the addition of calcium carbonate as a filler. The abrasion resistance of the underbody protection according to the invention according to Example 5 is even better than that of Comparative Example 6 according to the prior art.

It is particularly clear from the above examples that the use of sucrose in plastisol adhesives or sealants and underbody protection compositions enables the formulation of plastisols with very good properties.

Claims

claims

1. plastisol composition based on powdered organic polymers and plasticizers, characterized in that it contains powdered monosaccharides, disaccharides or oligosaccharides.

2. plastisol composition according to claim 1, characterized in that the powdery organic polymers are selected from the group formed by polyvinyl chloride, vinyl chloride copolymers with vinyl acetate, styrene and / or alkyl (meth) arylates, copolymers of styrene with (meth) acrylic acid, (meth) acrylamide and / or alkyl (meth) acrylates, copolymers of methyl or ethyl methacrylate with C _{3 to} C ₈ acrylic (meth) acrylates, alkyl methacrylate homopolymers or mixtures of the aforementioned polymers.

3. plastisol compositions according to claim 1 or 2, characterized in that the powdered monosaccharides, disaccharides or oligosaccharides are selected from glucose, galactose, mannose, fructose, arabinose, xylose, ribose, 2-deoxy-ribose, cellobiose, maltose (malt sugar), lactose (Milk sugar), sucrose (cane sugar), gentiobiose, melibiose, trehalose, turanose, gentianose, kestose, maltotriose, melecitose, raffinose, stachyose, lychnose, secalose or mixtures thereof.

4. plastisol compositions according to claim 3, characterized in that the mono-, di- or oligosaccharide (s) have an average particle size of 1 to 100 microns, preferably between 1 to 20 microns.

5. plastisol compositions according to at least one of the preceding claims, containing g) 5 to 60 wt.% Of at least one powdery polymer, h) 5 to 65 wt.% Plasticizer, i) 0 to 40 wt.% Fillers, j) 1 to 30 wt % of at least one mono-, di- or oligosaccharide k) 2 to 40% by weight of reactive additives, selected from the group of optionally blocked or microencapsulated di- or polyisocyanates; Amino- and / or hydroxy-functional additives, especially di- or polyamines or polyaminoamides, imidazole derivatives, epoxy resins, condensation products from epoxy resins and polyaminoamides and / or di- or polyamines, dicarboxylic acids di- or tricarboxylic acid anhydrides, acetylacetonates, peroxides or mixtures of the aforementioned reactive additives

I) if necessary, further auxiliaries and additives, the sum of the individual components being 100% by weight.

6. Use of a plastisol composition according to at least one of claims 1 to 5 in motor vehicle construction as an underbody protection agent, as an adhesive for the hood relining, as a mass for sill protection, as a metal adhesive, in particular as a seam seam adhesive

Flared seam sealing or as spot welding paste.